Liquid
Colourless
Clear
Amplification of standard template along with Taq DNA Polymerase, dNTP, corresponding primers should result in expected molecular size amplicon
Incubation at 37°C of the product with Plasmid DNA for 24 hours should show no degradation of the DNA
10X PCR Buffer (with MgCl2 ) is recommended for all PCR applications with Taq DNA Polymerases (both recombinant and native ).
10X PCR Buffer with 15mM Mg2+ – 4x1.25 ml
-20 °C (Blue/Dry Ice)
24 Months
Not Regulated for Transport (Non-Haz)
38229090 (GST 12%)
